Canonical Allele Identifier: CA458161935
Gene: TAS2R38 HGNC NCBI
OR9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.141673256A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141973456A>C , CM000669.2:g.141973456A>C GRCh38
NC_000007.13:g.141673256A>C , CM000669.1:g.141673256A>C GRCh37
NC_000007.12:g.141319725A>C NCBI36
NG_016141.1:g.5318T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000465654.5:c.-3+27459A>C ENSP00000419372.1:p.=
ENST00000547270.1:c.234T>G MANE Select ENSP00000448219.1:p.Leu78=
NM_176817.4:c.234T>G (TAS2R38) NP_789787.4:p.Leu78=
XM_011515783.1:c.*25-12940A>C (OR9A4) XP_011514085.1:p.=
NM_176817.5:c.234T>G (TAS2R38) MANE Select NP_789787.5:p.Leu78=